NDC 50771-201
Duloxetine Hydrochloride 20 mg capsule, delayed release pellets
On the label: Yaopharma Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yaopharma Co., Ltd. | Chongqing, China | Makes it | Problems found, fixed voluntarilyMar 29, 2019 · 3 inspections |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release pellets, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA207219
- On the market since
- Jan 1, 2024
- Package NDCs
50771-201-01- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
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